Cytotoxicity and Apoptotic Effects of Microcystin-LR and Anatoxin-a in Mouse Lymphocytes ( microcystin-LR / anatoxin-a / cytotoxicity / mouse lymphocytes / apoptosis )
Ivanka Teneva, Rumen D. Mladenov, Nikola Popov, Balik M. Dzhambazov
Abstract
Ivanka Teneva, Rumen D. Mladenov, Nikola Popov, Balik M. Dzhambazov
Abstract
There is an increasing amount of knowledge on the cytotoxic properties of cyanotoxins, but rela- tively little is known regarding their fine specificity and mechanisms of action. In this study, we investigated the influence of microcystin-LR and AnTx-a on mouse B- and T-lymphocyte subpopulations in vitro. Cyanotox- ins significantly decreased the cell viability after 4 and 24 h, compared to the untreated control. After 24 h exposure to microcystin-LR and anatoxin-a, the viabil- ity of splenocytes dropped to 23% and 57%, respec- tively. Our data demonstrate that microcystin-LR induced apoptosis specifically in mouse B cells, proba- bly via the B-cell antigen receptor and mitochondrial pathway, while the T cells were not affected. AnTx-a showed cytotoxic effects on both lymphocyte subpopu- lations, but the effects were driven by mechanisms dif- ferent from apoptosis. These findings demonstrate that the cyanotoxins could cause cytotoxic alterations in a variety of cell types different from the major targets, operating via distinct mechanisms.
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There is an increasing amount of knowledge on the cytotoxic properties of cyanotoxins, but rela- tively little is known regarding their fine specificity and mechanisms of action. In this study, we investigated the influence of microcystin-LR and AnTx-a on mouse B- and T-lymphocyte subpopulations in vitro. Cyanotox- ins significantly decreased the cell viability after 4 and 24 h, compared to the untreated control. After 24 h exposure to microcystin-LR and anatoxin-a, the viabil- ity of splenocytes dropped to 23% and 57%, respec- tively. Our data demonstrate that microcystin-LR induced apoptosis specifically in mouse B cells, proba- bly via the B-cell antigen receptor and mitochondrial pathway, while the T cells were not affected. AnTx-a showed cytotoxic effects on both lymphocyte subpopu- lations, but the effects were driven by mechanisms dif- ferent from apoptosis. These findings demonstrate that the cyanotoxins could cause cytotoxic alterations in a variety of cell types different from the major targets, operating via distinct mechanisms.
Key concepts: Cytotoxic T cell, Cytotoxicity, Apoptosis, Microcystin-LR, Biology, Microcystin, Splenocyte, Viability assay